What is NDC 68180-868?

68180-868 is the product NDC for Drospirenone And Ethinyl Estradiol kit, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Lupin Pharmaceuticals, Inc., NDC labeler code 68180. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Drospirenone And Ethinyl Estradiol?

12 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Drospirenone And Ethinyl Estradiol NDC 68180-868

NDC codes

FDA NDC Directory

Product NDC (as listed)68180-868Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68180-0868Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
68180-868-73	6818008687368180086873	3 POUCH in 1 CARTON (68180-868-73) / 1 BLISTER PACK in 1 POUCH / 1 KIT in 1 BLISTER PACK * 7 TABLET in 1 BLISTER PACK (68180-913-74) * 21 TABLET in 1 BLISTER PACK (68180-912-74)Marketed from Apr 15, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Drospirenone And Ethinyl Estradiol
Generic name (nonproprietary): drospirenone and ethinyl estradiol
Dosage form: Kit
Labeler: Lupin Pharmaceuticals, Inc.NDC labeler code 68180
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201663
Marketing start: Apr 15, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 68180-868_3c3a2ddd-8711-416c-813e-63c64f579ac2SPL ID 3c3a2ddd-8711-416c-813e-63c64f579ac2SPL set ID a8955f3b-afc9-4ef0-8946-9c97ab5b2e05RxCUI 284207, 748797, 748800

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N468180086873 followed by a unit qualifier and the quantity

Package 68180-0868-73. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 2, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Drospirenone and ethinyl estradiol tablet USP is a combination of drospirenone, a progestin, and ethinyl estradiol, an estrogen, indicated for use by females of reproductive potential to prevent pregnancy. ( 1 ) Drospirenone and ethinyl estradiol tablet USP is indicated for use by females of reproductive potential to prevent pregnancy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-868

What is NDC 68180-868?: 68180-868 is the product NDC for Drospirenone And Ethinyl Estradiol kit, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Drospirenone And Ethinyl Estradiol.
Who is the labeler?: Lupin Pharmaceuticals, Inc., NDC labeler code 68180. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Drospirenone And Ethinyl Estradiol?: 12 other product NDCs are listed under this name. See all Drospirenone And Ethinyl Estradiol NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Drospirenone And Ethinyl Estradiol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Drospirenone And Ethinyl Estradiol	—	Kit	Apotex Corp.	60505-4897	60505-4897-08
Drospirenone and Ethinyl Estradiol	—	Kit	NorthStar Rx LLC	72603-875	72603-0875-03
Drospirenone And Ethinyl Estradiol	—	Kit	Naari Pte. Limited	79929-019	79929-0019-07
Drospirenone And Ethinyl Estradiol	—	Kit	Redpharm Drug	67296-2286	67296-2286-03
Drospirenone and Ethinyl Estradiol	—	Kit	Camber Pharmaceuticals, Inc.	31722-945	31722-0945-3131722-0945-32
Drospirenone and ethinyl estradiol	—	Kit	Camber Pharmaceuticals, Inc.	31722-934	31722-0934-3131722-0934-32
drospirenone and ethinyl estradiol	—	Kit	A-S Medication Solutions	50090-2494	50090-2494-00
drospirenone and ethinyl estradiol	—	Kit	Glenmark Pharmaceuticals Inc., USA	68462-733	68462-0733-29
Drospirenone And Ethinyl Estradiol	—	Kit	Mylan Pharmaceuticals Inc.	0378-7300	00378-7300-53
drospirenone and ethinyl estradiol	—	Kit	A-S Medication Solutions	50090-2594	50090-2594-00

All 13 Drospirenone And Ethinyl Estradiol NDCs

Other NDCs under ANDA 201663

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 201663
Product	Strength	Form · route	Labeler	Product NDC
Drospirenone And Ethinyl Estradiol	—	Kit	Redpharm Drug	67296-2286